Implements a kernel-based association test for copy number variation (CNV) aggregate analysis in a certain genomic region (e.g., gene set, chromosome, or genome) that is robust to the within-locus and across-locus etiological heterogeneity, and bypass the need to define a "locus" unit for CNVs. Brucker, A., et al. (2020) <doi:10.1101/666875>.
|Author||Amanda Brucker, Shannon T. Holloway, Jung-Ying Tzeng|
|Maintainer||Shannon T. Holloway <email@example.com>|
|Package repository||View on CRAN|
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